JPH08320595A - Toner for two-component magnetic developer and developer - Google Patents

Abstract

PURPOSE: To obtain such a toner that an enough charge amt. of the toner can be maintained for development without compounding a negative charge controlling agent, movement of a charge controlling agent to the carrier surface and electrification defect due to spent of the toner are avoided, the electrification performance of the toner can be stabilized for a long time, lives of the toner and the carrier are prolonged, a wax component can be uniformly dispersed in the toner, and an image of stable image quality can be formed for a long time. CONSTITUTION: This toner is a negative charge two-component magnetic developer containing carbon black dispersed in a resin medium for fixing but no charge controlling agent compounded. The resin medium for fixing is a copolymer resin or a resin compsn. having radical or neutralized anionic polar groups. The wax used contains a polymer component produced by grafting. The carbon black used satisfies that pH<7 and (7-pH)/specific surface area (m<2> /g) ranging from 0.010 to 0.050 and is used by 4-15wt.% of the resin medium for fixing.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a toner for a two-component magnetic developer having excellent spent resistance, and more specifically, it does not contain a transferable charge control agent in toner particles, Moreover, toner does not scatter during development, and transfer is performed efficiently, so that a high-density image can be formed.
Toner and carrier life is also significantly extended.

[0002]

2. Description of the Related Art A so-called two-component magnetic developer is widely used as a developer for developing an electrostatic charge image formed on an electrophotographic photosensitive member.

This two-component magnetic developer is composed of a composition of a magnetic carrier composed of iron powder, ferrite particles and the like, and an electroscopic toner composed of a colored resin composition. At the time of development, by mixing a magnetic carrier and toner, the toner particles are charged to a constant polarity, the mixture is conveyed to the photoconductor in the form of a magnetic brush, and the surface of the photoconductor is rubbed with the magnetic brush. The charged toner is adsorbed and held on the charge image on the surface of the photoconductor to form a visible image.

In order to control the polarity of the toner particles due to triboelectric charging to a constant level, a charge control agent is generally contained in the toner particles. In the negatively chargeable toner, a metal-containing complex salt dye or a metal oxycarboxylic acid A negative charge control agent such as a complex (for example, JP-A-3-67268) is used, and in a positively chargeable toner, an oil-soluble dye such as nigrosine or a positive chargeability control agent such as an amine-based control agent (for example, JP-A No. 3-67268). 56-10624
No. 9) is used.

It has long been known to use a magnetic toner as a toner for a two-component magnetic developer, for example, in the above-mentioned JP-A-56-106249 or JP-A-59-162563. Describes using a magnetic powder internally added toner in which magnetic powder is contained in the toner,
On the other hand, Japanese Patent Application Laid-Open No. 3-67268 describes a magnetic powder externally added toner obtained by adding and mixing silica powder and magnetic powder to a toner base.

[0006]

The two-component magnetic developer is
It is known that at the initial stage of using the magnetic carrier and the toner mixed, even if the charging performance is satisfactory, the charging performance is deteriorated due to the generation of so-called spent (toner) and the life thereof is shortened. There is.

The spent (toner) is a phenomenon in which the toner component adheres to and deposits on the surface of the magnetic carrier in the form of a film. Since the surface of the magnetic carrier becomes closer to that of the toner, the triboelectrified series approaches. However, the predetermined charging performance cannot be obtained. Thus, the occurrence of spent has the disadvantage that the magnetic carrier must be discarded and replaced with a new magnetic carrier.

Therefore, an object of the present invention is to provide a negatively charged toner for a two-component magnetic developer which is excellent in spent resistance and has a long life of toner and carrier.

Another object of the present invention is to use no CCA (charge control agent) which does not contain a transferable charge control agent in the toner particles and can increase the apparent development sensitivity without toner scattering during development. Another object is to provide a negatively charged toner for a two-component magnetic developer.

Still another object of the present invention is to provide a negative component for a CCA-less two-component magnetic developer in which transfer from the surface of the photoconductor to paper is efficiently carried out even though it does not contain a transferable charge control agent. To provide charged toner.

[0011]

According to the present invention, in a negatively chargeable two-component magnetic developer toner in which carbon black is dispersed in a fixing resin medium, the fixing resin medium is free. Or a neutralized anionic polar group-containing copolymer resin composition containing a polymer component in which a wax is graft-fixed, and the carbon black has a pH of less than 7 and (7 -PH) /
A two-component magnetic developer having a specific surface area (m ² / g) in the range of 0.010 to 0.050 and being mixed in an amount of 4 to 15% by weight based on the fixing resin medium. An agent toner is provided.

According to the present invention, there is also provided a two-component magnetic developer comprising the above-mentioned toner and a resin-coated magnetic carrier or a magnetic carrier obtained by dispersing magnetic powder in a resin.

[0013]

The present inventors have found the following interesting facts in the course of repeated research to prevent toner spent generation.

FIG. 1 of the accompanying drawings shows that of a conventional two-component magnetic developer toner used for developing a positively charged image, a toner containing a chromium complex salt dye (2: 1 type) as a charge control agent is methanol. Extraction liquid wavelength of 200 to 700n
2 is a light absorption curve at m and has a peak in a wavelength range of 400 to 700 nm, and FIG. 2 shows a wavelength 2 of a methanol extract of a toner using a salicylic acid metal complex as a charge control agent.
It is an absorbance curve from 00 to 700 nm and has a wavelength of 280
It has a peak in the region of ˜350 nm.

According to these results, all the extraction liquids showed characteristic absorption peaks due to the charge control agent, which means that the surface of the toner particles contained the charge control agent in a considerably high concentration. ing. This is in good agreement with the idea that the charge control agent migrates to the surface of the toner particles even if it is internally added to the toner, and this migration controls the charge due to triboelectrification.

On the other hand, in FIG. 3, the toner used in the measurement of FIG. 1 was used as a two-component magnetic developer, and the carrier in which the charging failure was caused by the spent was similarly extracted with methanol. The absorbance curve at 200 to 700 nm is measured, and the wavelength is 400 to 70.
It has a peak in the region of 0 nm.

According to the measurement results, the charge control agent adheres to and deposits on the carrier surface in a high concentration, and the charging failure due to the spent is not the mere filming of the carrier surface due to the toner resin, which has been considered in the past. The surprising fact of migration of the control agent to the carrier surface was revealed.

This fact becomes more apparent with reference to FIGS. 4 and 5. FIGS. 4 and 5 show the mixing time and the spent amount when a mixture of a toner containing a positive or negative charge control agent and a magnetic carrier and a mixture of a toner containing no charge control agent and a magnetic carrier were mixed. And the relationship between the mixing time and the charge amount are plotted. From these results, it becomes clear that in the case of containing the charge control agent, the amount of spent increases as the mixing time increases, and the decrease in the amount of charge increases.

Further, FIG. 6 shows the relationship between the amount of spent spent carrier and the charge control agent in the spent toner, and the dotted line in FIG. 6 indicates the predicted value calculated from the toner prescription. It is a plot. According to this result, it becomes clear that the charge control agent is selectively transferred to and adheres to the carrier surface in the early stage of spent generation. Incidentally, in the result of FIG. 6, the reason why the charge control agent amount is close to the predicted value from the composition with the increase of the spent amount is the result of the above-mentioned mixed system in the closed system without toner replenishment. Therefore, when the toner is replaced in the copying machine, it can be expected that the difference due to the presence or absence of the charge control agent is further widened.

Furthermore, FIG. 7 shows the relationship between the mixing time and the amount of spent when the individual components in the toner are mixed with the magnetic carrier. According to this result, it was clarified that the charge control agent is a component that easily migrates to the carrier surface among the respective components in the toner and easily causes spent.

From the above, the charging failure due to the spent generation in the conventional two-component magnetic developer, as shown in the explanatory view of FIG.
Also, the toner is negatively charged, but as the spent is formed by the selective transfer of the charge control agent on the carrier surface, the spent layer is negatively charged and a positive polarity opposite polarity toner is formed. Can possibly be explained.

In the present invention, in order to prevent migration of the charge control agent to the surface of the magnetic carrier, the internal addition or blending of the migration charge control agent to the toner particles is stopped. Along with this,
As shown in the absorbance curve of FIG. 9, the negatively chargeable toner of the present invention has a substantially zero absorbance at a wavelength of 400 to 700 nm even when extracted with methanol. Of course, the toner of the present invention does not have a positive charge control agent such as a salicylic acid metal complex, and therefore does not have a peak of absorbance at a wavelength of 280 to 350 nm of the methanol extract. In the present specification, the absorbance being substantially zero means that an absorption peak in the above wavelength region is not detected at all in an extract obtained by extracting 0.1 g of toner with 50 ml of methanol, or even if it is detected, the absorbance at that peak is detected. Is less than or equal to 0.05.

By the way, as shown in FIG. 5, the toner containing no charge control agent has an insufficient charge amount as compared with the toner containing the charge control agent. In the present invention,
In order to prevent this, a copolymer resin composition having an anionic polar group is used as the fixing resin medium, and carbon black as a colorant having a pH on the acidic side is used. By using such a fixing resin medium and carbon black, the amount of toner charge required for development can be obtained.

That is, the anionic polar group contained in the fixing resin medium imparts a negative charging property to the toner, and since this polar group exists in the molecular skeleton of the resin, it appears as a charge control agent. In addition, they do not migrate to the particle surface of the carrier and cause spent. The fixing resin medium used in the present invention has an acid value in relation to having an anionic polar group as described above, and this acid value is in the range of 4 to 30. is necessary. That is, when the acid value is greater than 30, the amount of anionic groups increases, and the hygroscopicity of the toner itself increases, making it difficult to perform stable triboelectric charging. When the acid value is lower than 4, the amount of anionic groups is small and it is difficult to secure a sufficient toner charge amount for development. still,
This anionic polar group may be present in the form of a free acid, or may be present in the form of a metal salt such as sodium salt, that is, in a neutralized form, and the acid value is measured in the form of the free acid. To be done. That is, in the present invention, the acid value is a value measured in the form of a free acid by hydrolyzing at least a part of the anionic polar group when it exists in a neutralized state. .

In the present invention, the fixing resin medium described above contains a polymer component to which wax is graft-fixed. That is, the wax is grafted to the above-mentioned copolymer having an anionic polar group, or is grafted to a polymer different from the copolymer resin having an anionic polar group and blended with the copolymer resin. Existing in the fixing resin medium.

In general, a releasing agent such as wax is added to the toner in order to improve offset resistance. However,
The wax blended as a release agent has an SP value (solubility parameter) greatly different from that of the fixing resin medium, and thus it is difficult to uniformly disperse the wax in the medium, and the wax content of each toner particle varies. There is a problem that the wax is generated or the wax is unevenly distributed on the surface of the toner particles. That is, when developing with such a toner, wax easily adheres to the surface of the carrier particles as a spent, and when a developer formed by mixing the toner particles and the carrier particles is used for a long period of time, the spent carrier The chargeability of the particles decreases, and durability becomes a problem.

In the present invention, the wax is introduced as a graft chain into the polymer constituting the fixing resin medium to improve the uniform dispersibility of the wax.
That is, since the wax-grafted polymer can be easily dispersed evenly in the fixing resin medium in the form in which the wax components are bonded, the wax is prevented from adhering to the surface of the carrier particles as spent as much as possible. Therefore, the life of the developer can be extended.

Further, according to the present invention, as described above, the carbon black as a colorant has a pH on the acidic side (that is, less than 7) and (7-pH) / specific surface area (m ² / m ² ). It is important to use those whose ratio g) is in the range of 0.010 to 0.050. Generally, carbon black has a pH of about 8 and is biased toward neutral or alkaline side. In addition, in order to control the conductivity, carbon black that is acid-treated to have a pH of less than 7 is also known. In the present invention, carbon black having a pH of less than 7 is selectively used, but this does not mean that carbon black whose conductivity is controlled is used.

According to the research conducted by the present inventors, it was confirmed that the carbon black was negatively charged when the carbon black and the magnetic carrier were mixed and stirred. That is, in the present invention, by using the carbon black which has been treated with an acid and has a pH of less than 7, the negative chargeability of the fixing resin medium having the anionic polar group is reinforced, and the negative charge control agent is used. It is possible to effectively prevent the deterioration of the charging property due to the unblended.

In the present invention, the above-mentioned (7-pH) /
The value of the specific surface area is the degree of acid treatment, that is, an index showing the density of acid functional groups present on the surface of carbon black. If this value is smaller than the above range, the negative charging property is not sufficiently reinforced, Inevitably, the chargeability is reduced. On the other hand, when it is larger than the above range, the hygroscopicity of the toner becomes high, and it becomes difficult to secure a stable triboelectric charge amount.

The pH of carbon black was 5 g for a sample.
Can be boiled for 5 minutes in 100 ml of ion-exchanged water, allowed to cool, supplemented with evaporated water and filtered through filter paper, and the filtrate can be measured with a commercially available glass electrode pH meter.

[0032]

Preferred Embodiment of the Invention

(Fixing Resin Medium) The fixing resin medium used in the present invention comprises a resin composition containing a copolymer resin having an anionic polar group and a wax-grafted polymer component.

In the above-mentioned copolymer resin, the anionic polar group may be any polar group such as carboxylic acid, sulfonic acid and phosphonic acid, and the carboxylic acid type is particularly preferable. The copolymer resin having such an anionic polar group is one in which the monomer having the polar group is incorporated into the resin by random copolymerization, block copolymerization, graft copolymerization or the like. Suitable examples of such monomers are as follows.

Examples of the carboxylic acid type include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, maleic anhydride, fumaric acid, maleic acid and fumaric acid. Etc.

Examples of the sulfonic acid type include styrene sulfonic acid and 2-acrylamido-2-methylpropane sulfonic acid.

Examples of the phosphonic acid type include 2-acid phosphoxypropyl methacrylate, 2-acid phosphoxyethyl methacrylate, 3-chloro-2-acid phosphoxypropyl methacrylate and the like.

These anionic polar group-containing monomer units are neutralized with free acids, alkali metals such as sodium and potassium, alkaline earth metals such as calcium and magnesium, zinc and the like. It may be incorporated in the form.

The other monomer which is the main component of the copolymer resin is one in which the produced polymer has the fixability and the chargeability required for the toner, and is one of the monomers having an ethylenically unsaturated bond. One kind or a combination of two or more kinds is used.

Suitable examples of such a monomer include acrylic acid ester monomers, monovinyl aromatic monomers, vinyl ester monomers, vinyl ether monomers, diolefin monomers, Monoolefin-based monomers and the like. Specifically, the following can be exemplified. still,
In the following description, the lower alkyl group means a group having 5 or less carbon atoms.

Examples of the acrylate monomer include the following general formula (1): CH ₂ ═C (R ¹ ) —COOR ² (1) In the formula, R ¹ is a hydrogen atom or a lower alkyl group, and R ^{2 is} Is an alkyl group having 11 or less carbon atoms or 12 or more carbon atoms, or a hydroxyalkyl group having 11 or less carbon atoms, for example, methyl acrylate, ethyl acrylate, butyl acrylate, acrylic acid-2- Ethylhexyl, cyclohexyl acrylate, phenyl acrylate,
Methyl methacrylate, hexyl methacrylate, 2-ethylhexyl methacrylate, ethyl β-hydroxyacrylate, γ-hydroxypropyl acrylate, δ-hydroxybutyl acrylate, β-hydroxyethyl methacrylate, and lauryl acrylate, acrylic acid Tridecyl, stearyl acrylate, docosyl acrylate, dicyclohexylmethyl acrylate, dicyclohexylpropyl acrylate, cyclododecyl acrylate, cycloundecanemethyl acrylate, lauryl methacrylate,
Examples thereof include tridecyl methacrylate, stearyl methacrylate, docosyl methacrylate, dicyclohexylmethyl methacrylate, dicyclohexylpropyl methacrylate, cyclododecyl methacrylate, cycloundecane methyl methacrylate and the like.

Examples of the monovinyl aromatic monomer include the following general formula (2): CH ₂ = C (R ³ ) -Φ-R ⁴ (2) In the formula, R ³ is a hydrogen atom, a lower alkyl group, or a halogen. Is an atom or an alkyl group having 12 or more carbon atoms, R ⁴ is a hydrogen atom, a lower alkyl group, an alkyl group having 12 or more carbon atoms, a halogen atom, an alkoxy group, an amino group, a nitro group, and Φ is a phenylene group. , A lower alkyl group as a substituent, an alkyl group having 12 or more carbon atoms, a halogen atom,
Those having an alkoxy group, an amino group or a nitro group, represented by, for example, styrene, α-methylstyrene, vinyltoluene, α-chlorostyrene, o-, m
-, P-chlorostyrene, p-ethylstyrene, as well as m- or p-laurylstyrene, m- or p-stearylstyrene, α-methyl-3-stearylstyrene, m
-Or p-stearoxystyrene, 4-vinylbenzoic acid stearyl, 4-stearoylaminostyrene and the like can be mentioned.

Examples of the other monomer include those represented by the following general formula (3), (4), (5) or (6). CH in ^{_{2 = CH-OOCR 5 (3}} ) formula, R ⁵ is a hydrogen atom, a lower alkyl group, or 1 carbon atoms
A vinyl ester represented by the formula of 2 or more alkyl groups, such as vinyl formate, vinyl acetate, vinyl propionate, and vinyl laurate, vinyl tridecanoate, vinyl stearate, vinyl docosanoate, vinyl triacontanate, pentylcyclohexane. Vinyl acetate, dicyclohexyl vinyl acetate, etc.

CH ₂ ═CH—O—R ⁶ (4) In the formula, R ⁶ is an alkyl group having 11 or less carbon atoms or 12 or more carbon atoms, such as vinyl ether, for example vinyl methyl ether, vinyl ethyl ether. , Vinyl-n
-Butyl ether, vinyl phenyl ether, vinyl cyclohexyl ether, vinyl lauryl ether, vinyl stearyl ether, vinyl docosyl ether, vinyl cyclododecyl ether, etc.

CH ₂ ═C (R ⁷ ) —C (R ⁸ ) ═CH—R ⁹ (5) In the formula, each of R ⁷ , R ⁸ , and R ⁹ is a hydrogen atom, a lower alkyl group, or a carbon number of 12 or more. An alkyl group or a halogen atom, a diolefin such as butadiene, isoprene, chloroprene, and 1,3-hexadecadiene,
1,3-docosadiene, 2-methyl-1,3-docosadiene and the like.

CH ₂ ═C (R ¹⁰ ) —R ¹¹ (6) In the formula, each of R ¹⁰ and R ¹¹ is a hydrogen atom, a lower alkyl group, or an alkyl group having 12 or more carbon atoms, Classes, especially ethylene, propylene, isobutylene, butene-1, pentene-1, 4-methylpentene-1, as well as 1-tetradecene, 1-eicosene and the like.

In the present invention, the anionic polar group in the above-mentioned copolymer resin has an acid value of 4 to 3 in the fixing resin medium.
It is preferably present in an amount of 0, especially 5 to 15. When part or all of the anionic polar group of the copolymer resin is neutralized, the content of the anionic polar group corresponding to the acid value including the polar group of the neutralized part is adjusted. It is better to have one. That is, when the acid value of the fixing resin medium is smaller than the above range, the amount of the anionic polar group is small and the chargeability of the toner tends to be unsatisfactory. On the other hand, when it is larger than the above range, the toner becomes humidity sensitive. The chargeability of the toner is also unsatisfactory, which is not preferable.

In order to further improve the uniform dispersibility of the wax-grafted polymer component described below and prolong the life of the developer, the monomers of the above formulas (2) to (6) are used. Among them, a copolymer resin in which one having an alkyl group having 12 or more carbon atoms is used as one of the monomer components is preferable. For example, as the monovinyl aromatic monomer of the formula (2), R ³ or R ⁴ is an alkyl group having 12 or more carbon atoms, or phenylene group Φ is an alkyl group having 12 or more carbon atoms as a substituent. In the vinyl ester of the formula (3), R ⁵ is an alkyl group having 12 or more carbon atoms, and in the vinyl ether of the formula (4), R ⁶ is 1 carbon atom.
At least one of R ⁷ , R ⁸ and R ^{9 in} the diolefins of formula (5) having 2 or more alkyl groups has 1 carbon atom
In the case of two or more alkyl groups, and in the monoolefins of the formula (6), at least one of R ¹⁰ and R ¹¹ has 1 carbon atom.
Those having two or more alkyl groups are preferable. These alkyl groups having 12 or more carbon atoms are introduced into the side chains of the polymer chain, and in order to effectively exhibit the effects such as improvement in durability, they have such long-chain alkyl groups. The amount of the monomer is 0.1 to 20 parts by weight based on the total amount of the monomer, and especially 0.1.
It is preferably used in an amount of 5 to 10 parts by weight.

In the present invention, a suitable copolymer resin contains, as an essential component, an anionic polar group-containing monomer and one or more of the acrylic monomers of the formula (1). Copolymer resins containing the monomers of formulas (2) to (6) can be mentioned, and the most preferable one is styrene-acrylic copolymer resin. Taking a copolymer resin having an alkyl group having 12 or more carbon atoms in its side chain as an example, styrene- (meth) acrylic acid-stearyl (meth) acrylate copolymer, styrene- (meth) acryl are specific examples. Acid ester- (meth) acrylic acid stearyl- (meth) acrylic acid copolymer, styrene-
Examples thereof include stearyl (meth) acrylate- (meth) acrylic acid copolymer and styrene-stearyl (meth) acrylic acid-maleic acid copolymer.

The fixing resin medium of the present invention contains a wax-grafted polymer component together with the above-mentioned copolymer resin containing anionic polar groups. As described above, since the wax is fixed as the graft chain of the polymer, it is possible to disperse the wax uniformly with the copolymer resin, and it is possible to ensure the extension of the developer life.

As the wax to be graft-fixed, various natural or synthetic waxes can be used. In general, polyolefin waxes such as polypropylene wax, polyethylene wax and propylene-ethylene random copolymer wax are used. Used,
Polypropylene wax is particularly preferable. Further, such a wax is 0.01 to 10 parts by weight per 100 parts by weight of the fixing resin medium in a state where the wax is not fixed by grafting,
In particular, it is used in an amount of 0.1 to 6 parts by weight. If this amount is smaller than the above range, the offset resistance becomes unsatisfactory, and if it is used in a larger amount than the above range, the toner chargeability decreases and toner scattering, fog, etc. easily occur due to poor charging. Become.

Graft fixing of such a wax can be easily carried out, for example, by radical polymerization in the presence of wax when the copolymer resin having an anionic polar group is synthesized by radical polymerization. That is, the wax is graft-fixed on a part of the copolymer having an anionic polar group, whereby the wax can be graft-fixed simultaneously with the production of the copolymer resin.
Needless to say, the wax may be graft-fixed completely separately from the above-mentioned copolymer resin containing an anionic polar group.
That is, a wax graft fixing polymer is included by radically polymerizing a monomer having no anionic polar group, for example, at least one of the monomers of the above formulas (2) to (6) in the presence of wax. Since a resin or a copolymer resin is obtained, it may be blended with a copolymer resin containing an anionic polar group.

The fixing resin medium used in the toner of the present invention contains the above-mentioned anionic polar group-containing copolymer resin and the wax graft fixing polymer component.
The copolymer resin may be contained alone or in combination of two or more kinds. Further, it goes without saying that it may be used in the form of a composition with a polymer component other than these,
Also in this case, it is preferable to set the acid value and the wax content in the ranges described above.

In the present invention, the above-mentioned fixing resin medium has a weight average molecular weight of 70,000 to 200,000, particularly 80,000 to 150,000 in order to ensure a certain pulverizability and granulation. Is preferable, and the molecular weight peak is 4,000 to 3
It is preferable to contain a low molecular weight component having a molecular weight peak in the range of 10,000, particularly 6,000 to 20,000, and a high molecular weight component having a molecular weight distribution in a higher molecular weight region than this. That is, the low-molecular component improves the heat fixing property of the toner, and the high-molecular component improves the offset resistance. From the viewpoints of uniform dispersibility of the high molecular component and the low molecular component and the transfer efficiency, the low molecular component is preferably contained in an amount of 40 to 75% by weight based on the fixing resin medium. The above-mentioned anionic polar group may be introduced into either the low molecular weight component or the high molecular weight component, or may be introduced into both, as long as the acid value of the resin medium is within the above range. .

(Manufacturing Method of Fixing Resin Medium) The above-mentioned fixing resin medium uses the above-mentioned monomer component, and radical polymerization is carried out using a polymerization initiator known per se in the presence of wax. It can be easily manufactured by carrying out. In this case, the fixing resin medium containing the low-molecular component and the high-molecular component described above is prepared by previously producing the low-molecular component,
This can be obtained by blending with a separately produced polymer component or by carrying out radical polymerization in the presence of this low molecular component to produce a polymer component. Generally, from the viewpoint of uniform dispersibility of the high molecular component and the low molecular component, it is desirable to produce the high molecular component in the presence of the low molecular component. The wax may be fixed by grafting at any stage of production of the low molecular weight component and the high molecular weight component.

A specific example of this production method is as follows, using a specific monomer component as an example. First, styrene, acrylic acid or methacrylic acid, an acrylic acid ester having an alkyl group having 12 or more carbon atoms, a polymerization initiator and a wax, for example, both a monomer component such as toluene and xylene, and a forming polymer component. Mix in a soluble organic solvent and stir. This mixed solution is put into a reaction kettle and stirred well at 60 to 250 ° C. and 3 to
Polymerization and wax grafting for about 10 hours,
After completion of the polymerization, the solution is degassed and dried to obtain a polymer as a low molecular weight component. Next, similarly, in a solvent, styrene, acrylic acid or methacrylic acid, an acrylic acid ester, the polymer for a low molecular weight component obtained above and a polymerization initiator are mixed and stirred. This mixed solution is put into a reaction kettle and polymerized at 60 to 200 ° C. for about 5 to 24 hours while stirring well, and after the polymerization is completed, the solution is degassed and dried to fix the desired wax graft. A fixing resin medium containing a polymer component and also containing a low molecular component and a high molecular component can be obtained. The acid value can be easily adjusted by adjusting the charged amount of the anionic polar group-containing monomer.

(Carbon black) In the present invention, the carbon black dispersed in the fixing resin medium has a pH of less than 7, preferably 2 to 5, and (7-pH) / specific surface area. (M ² / g) is 0.0
As long as it is in the range of 10 to 0.050, particularly 0.015 to 0.040, any one can be used, but in general, furnace black is used, and the above treatment is carried out by acid treatment. Those adjusted to have a pH value satisfying the above conditions are preferable. Acid treatment
For example, it can be carried out by using an inorganic acid such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid or the like, and an organic acid such as acetic acid, citric acid, propionic acid, benzoic acid, salicylic acid, toluenesulfonic acid, etc. An acidic group such as a group is introduced to reinforce the negative chargeability of the toner. Further, the amount of acid used for the treatment is extremely small, as is clear from the above pH conditions, so that this does not adversely affect the electrical characteristics of the toner.

The specific surface area of such carbon black is usually 50 m ² / g or more, particularly 100 to 300.
It is preferably in the range of m ² / g from the viewpoint of dispersibility in the resin. Such carbon black is contained in the fixing resin medium in an amount of 4 to 15% by weight, particularly 6 to 1% by weight.
It is compounded in an amount of 2% by weight. If the blending amount is less than the above range, the negative chargeability of the toner becomes unsatisfactory and fogging and the like are likely to occur. If it is used in a larger amount than the above range, the fixability of the toner will deteriorate.

(Other Compounding Agents) In the two-component magnetic developer toner of the present invention, other than the above carbon black, other than the above-mentioned carbon black, various known toner mixing agents are known. An agent such as an extender pigment may be dispersed and compounded in the fixing resin medium.

Examples of extender pigments include barite powder, barium carbonate, clay, silica, white carbon, talc, and alumina white. Such pigments are used in an amount of 2 to 20 parts by weight, especially 5 to 15 parts by weight, per 100 parts by weight of the fixing resin medium.

In the present invention, the wax is graft-fixed to the polymer component in the fixing resin medium. However, various waxes may be blended alone or in combination of two or more as long as the object of the present invention is not impaired. It is possible to do so.

In the present invention, in addition to the above-mentioned respective compounding agents, for example, magnetic powder may be dispersed and compounded in the fixing resin medium. By blending such magnetic powder, the toner particles in the magnetic brush at the time of development are held by the carrier not only by the Coulomb force but also by the magnetic attraction force, so that the toner scattering can be prevented more reliably, and the toner of the copying machine can be more reliably prevented. It is extremely preferable from the viewpoint of preventing toner contamination and fogging of copied materials. Such advantages are required as the copying speed increases. The addition of such magnetic powder also has the advantages that the amount of charge per toner particle can be reduced, the development sensitivity can be improved, and a high-density image can be obtained.

Examples of such magnetic powders include magnetic powders conventionally used in magnetic toners, for example, ferric tetroxide (Fe ₃ O).
₄ ), ferric oxide (γ-Fe ₂ O ₃ ), zinc iron oxide (Z
nFe ₂ O ₄ ), yttrium iron oxide (Y ₃ Fe
₅ O ₁₂ ), iron cadmium oxide (CdFe ₂ O ₄ ), iron gadolinium oxide (Gd ₃ Fe ₅ O ₁₂ ), iron oxide copper (CuF)
e ₂ O ₄ ), lead iron oxide (PbFe ₁₂ O ₁₉ ), iron nickel oxide (NiFe ₂ O ₄ ), iron neodymium oxide (NdFe)
O ₃ ), iron oxide barium (BaFe ₁₂ O ₁₉ ), iron oxide magnesium (MgFe ₂ O ₄ ), iron manganese oxide (Mn
Fe ₂ O ₄ ), lanthanum iron oxide (LaFeO ₃ ), iron powder (Fe), cobalt powder (Co), nickel powder (Ni),
Etc. can be mentioned. A particularly suitable magnetic powder is fine particle triiron trioxide (magnetite). The preferred magnetite has a regular octahedron shape and a particle size of 0.05 to 1.0 μm. The magnetite particles may be surface-treated with a silane coupling agent, a titanium coupling agent, or the like.

The compounding amount of the above-mentioned magnetic powder is the resin medium 10
It may be as small as 0.1 to 5 parts by weight, especially 0.5 to 3.0 parts by weight, per 0 parts by weight. Conventionally, the magnetic toner used for the one-component magnetic developer uses the magnetic powder in an amount of more than 10 parts by weight per 100 parts by weight of the resin medium, but the amount of the magnetic powder used above is considerably smaller than this. With such a small amount of internal addition, it is possible to form a high-density image while preventing toner scattering.

(Toner) The toner of the present invention can be produced by a method known per se such as a pulverizing and classifying method, a melt granulating method, a spray granulating method and a polymerization method, but the pulverizing and classifying method is general. That is, the above-mentioned fixing resin medium and various toner compounding agents are pre-mixed with a mixer such as a Henschel mixer, and then kneaded using a kneading device such as a twin-screw extruder, and after cooling the kneaded composition, It is crushed and classified to obtain a toner.
The particle size of the toner is preferably such that the volume-based average particle size (median size by Coulter counter) is in the range of 5 to 15 μm, particularly 7 to 12 μm.

If necessary, a fluidity improver such as hydrophobic vapor phase silica may be externally added to the surface of the toner particles to improve the fluidity of the toner. Such a fluidity improver is usually an extremely fine powder having a primary particle size of about 0.005 to 0.050 μm, and is based on the total weight of the toner (that is, the total amount of the above-mentioned toner particles and external additives). It is preferable to add externally in an amount of 0.1 to 2.0% by weight.

According to a preferred embodiment of the present invention, together with the fluidity improver, the particle size is larger than that of the fluidity improver by 0.0.
Spacer particles having a particle size of 5 to 1.0 μm, particularly 0.07 to 0.5 μm are externally added to the toner particles. That is, by externally adding such spacer particles, the bond between the toner image and the latent image on the surface of the photoconductor is weakened so that the toner image can be easily peeled off. The transfer efficiency can be improved.

As the spacer particles, organic or inorganic inert particles having the above particle size can be used. Specific examples of such inert fixed particles include silica, alumina, titanium oxide, magnesium carbonate, acrylic resin powder, styrene resin powder, and magnetic powder, but in general, the above-mentioned magnetic powder, particularly fine particles. Preference is given to using ferrosoferric oxide (magnetite). This is because the magnetic powder existing on the surface of the toner particles also effectively acts on the toner scattering. Such spacer particles may be externally added in an amount of 10% by weight or less, preferably 0.1 to 10% by weight, and most preferably 0.1 to 5% by weight based on the total weight of the toner. When used in excess of this, the image density is reduced. When magnetic powder is used as the spacer particles, when the magnetic powder is internally added to the toner particles, the total amount of the magnetic powder and the internally added magnetic powder is 10% by weight or less based on the fixing resin medium. Is good. This is because, if this total amount becomes excessive, the image density will also decrease.

When the fluidity-improving agent and the spacer particles are externally added to the toner, the fluidity-improving agent and the spacer particles are previously intimately mixed under a pulverizing condition, and this mixture is added to the toner to sufficiently disintegrate the toner. Good to do. As a result, these external additives adhere to the surface of the toner particles, that is, are held in contact with the surface of the toner particles or fixed in a state where they are partially driven into the surface of the particles.

(Magnetic Carrier) As the magnetic carrier particles used in combination with the above-mentioned toner, those known per se can be used, but the following formula (7): MOFe ₂ O ₃ (7) is preferable. In the formula, M is Cu, Zn, Fe, Ba, Ni, Mg, M
a magnetite (M = F) which is at least one metal selected from the group consisting of n, Al and Co.
e), ferrite (M is other than Fe), and among them, M is at least one of Cu, Zn, Mg, Mn, and Ni, preferably a soft ferrite containing two or more, for example, copper-zinc-magnesium ferrite. Sintered ferrite particles, especially spherical particles are preferred.

Since these magnetic carrier particles show little change in electrical resistance due to environmental changes or changes over time, they exhibit stable charging properties, and the magnetic brush has soft ears.
It is advantageous in that it does not generate white streaks such as a trace of a magnetic brush on the formed image. The average particle size of the magnetic carrier is generally 30 to 200 μm.
, Especially 50 to 150 μm, and the saturation magnetization is 30 to 70 emu / g, especially 45 to 65
emu / g and volume resistivity of 10 ^{5 to} 10 ⁹ Ω · c
m, especially in the range of 10 ^{6 to} 10 ⁸ Ω · cm.

Further, the magnetic carrier particles can be used by coating them with various kinds of thermoplastic resins or thermosetting resins, using the core as the core. For example, as the thermoplastic resin, there is a thermoplastic acrylic resin, a thermoplastic styrene-acrylic resin, a polyester resin, a polyamide resin, an olefin copolymer resin, or the like, and as the thermosetting resin, a modified or unmodified silicone resin, Examples include thermosetting acrylic resin, thermosetting styrene-acrylic resin, phenol resin, urethane resin, thermosetting polyester resin, epoxy resin, amino resin, fluororesin, and melamine resin. With such a resin coat, the occurrence of spent can be more effectively avoided. Generally speaking, the amount of resin coating is preferably 0.001 to 2.5 parts by weight, and more preferably 0.005 to 2.0 parts by weight, based on 100 parts by weight of the core particles.

In the present invention, it is preferable to introduce a cationic polar group into the above coating resin. That is, by providing the resin coating layer having a cationic polar group, the positive charging property of the carrier is improved, and thus the negative charging property of the toner can be further improved. Such cationic polar groups include basic nitrogen-containing groups such as primary, secondary or tertiary amino groups, quaternary ammonium groups, amide groups, imino groups, imide groups, hydrazino groups,
Typical examples are guanidino group and amidino group, and amino group and quaternary ammonium group are particularly preferable.

The introduction of the cationic polar group may be carried out, for example, by using the above-mentioned cationic group-containing monomer as a monomer component to produce a resin, and by using a silane coupling agent having a cationic group. It can also be introduced by subjecting the resin to a surface treatment. As such a silane coupling agent, N-β (aminoethyl) γ-aminopropyltrimethoxysilane, N-β (aminoethyl) γ-aminopropylmethyldimethoxysilane, γ-aminopropyltriethoxysilane, N- Phenyl-γ-aminopropyltrimethoxysilane and the like. Furthermore, the cationic polar group can be introduced into the resin by synthesizing the above coated resin by polymerization using a polymerization initiator having a cationic polar group such as an amidine type azobis compound. The amount of these cationic polar groups is generally in the range of 0.1 to 2000 mmol, particularly 0.5 to 1500 mmol, per 100 g of resin.

It is of course possible to mix various additives known per se in the resin coating layer, if necessary, such as silica, alumina, carbon black, fatty acid metal salts, silane coupling agents and silicone oil. Is.

The resin coating of the carrier particles to be the core is
It can be carried out by a method known per se, for example, by dissolving the above-mentioned coat resin in a suitable solvent and using this resin solution, a dipping method, a spray method, a fluidized bed method, a moving bed method, a rolling bed method, etc. Thus, resin coating can be performed. When the thermosetting resin is coated, the resin may be cured by heating or the like after the coating is performed by the above method using a solution of an uncured resin or an oligomer.

In the present invention, it is also possible to use a binder type carrier formed by dispersing magnetic powder in a binder resin. As such a magnetic powder, the above-mentioned magnetic powder, particularly magnetite, can be preferably used, and the particle size thereof is 2.0 μm or less, particularly 0.05 to 1.0 μm.
It should be in the range of. This magnetic powder is a binder resin 100
150 to 900 parts by weight, especially 250 to 6 parts by weight
It is preferably used in an amount of 00 parts by weight.

As the binder resin, a thermoplastic resin,
Examples of thermosetting resins in the form of uncured or initial condensate, such as vinyl aromatic resins such as polystyrene, acrylic resins, polyvinyl acetal resins, polyester resins, epoxy resins, phenol resins, petroleum resins, polyolefin resins, etc. it can. Among these, styrene resins, acrylic resins, and styrene-acrylic copolymer resins are preferable.

The binder type carrier may be blended with an auxiliary agent known per se, such as carbon black for controlling electric resistance, a dispersant, a dispersion auxiliary agent, a low molecular weight or high molecular weight charge control agent and the like. it can. Similarly to the above, a cationic polar group may be introduced to enhance the positive charging property of the carrier and improve the negative charging property of the toner. Even in such a binder type carrier, the average particle size and the like are preferably in the same range as the above-mentioned carrier.

(Two-Component Magnetic Developer) The toner of the present invention is used as a magnetic developer by mixing with the above-mentioned various magnetic carriers, and the mixing ratio of these carriers and toner is generally 98. : 2 to 90:10 weight ratio, especially 97: 3 to 94: 6 weight ratio.

In the electrostatographic copying method using such a two-component magnetic developer, the electrostatic latent image can be formed by any method known per se. After uniformly charging the conductive layer, it can be imagewise exposed to form an electrostatic latent image. Development of the electrostatic image is easily performed by bringing a magnetic brush of a two-component magnetic developer into contact with the substrate. The toner image formed by the development is transferred onto a copy sheet, and the toner image is fixed by bringing it into contact with a heating roll.

[0081]

DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described with reference to the following examples.

(Evaluation of Developers) The developers and toners obtained in the following Examples and Comparative Examples were evaluated by using each developer as a copying machine manufactured by Mita Kogyo (trade name "DC-4086" modified machine). ), And made a copy of the following items.

(A) Transfer efficiency: The amount of toner in the toner hopper before the start of copying and the amount in the toner hopper after copying a predetermined number of sheets were measured, and the toner consumption amount was calculated from the difference. On the other hand, the amount of toner collected in the cleaning process during the copying of a predetermined number of sheets was measured to obtain the amount of toner collected.
From these values, the transfer efficiency of toner was calculated by the following formula. The copy original used for copying was a character original having a black area ratio of 8%. Transfer efficiency (%) = [(A−B) / A] × 100 In the formula, A represents the toner consumption amount and B represents the toner recovery amount.

(B) Image density (ID): Copying was performed using a character original having an area ratio of black portion of 8%, and copying was continued until the transfer efficiency was less than 70%. The reflection densitometer (model number "TC
-6D "manufactured by Tokyo Denshoku Co., Ltd.). The original used for sampling every 5,000 sheets has an area ratio of black portions including black solid portions of 15%.

(C) Fog Density (FD) Copying was performed using a character original having an area ratio of black portion of 8%.
Copying was continued until the transfer efficiency was less than 70%. The density of the black solid part of the sampled image was measured every 5,000 sheets using the same reflection densitometer as described above. The difference between this measurement value and the measurement value obtained by measuring the paper base paper before copying with a reflection densitometer was calculated, and the maximum value was defined as the fog density (FD). still,
The manuscript used for sampling every 5,000 sheets is
The area ratio of the black part including the black solid part is 15%.

(D) Resolution Copying is performed using a character original having an area ratio of the black portion of 8%.
At the time of copying 50,000 sheets (when the transfer efficiency is less than 70% by then), the specified chart original (1
A copy was made using a document in which a predetermined number of parallel straight lines were drawn within the width of mm, and the obtained copy image was evaluated by visual judgment.

(E) Charge amount Copying is performed using a character original having an area ratio of black portion of 8%.
Copying was continued until the transfer efficiency was less than 70%. Every time 5,000 copies were made, the charge amount of 200 mg of the developer was measured using a blow-off powder charge amount measuring device (manufactured by Toshiba Chemical Co.), and the average value of the charge amount per 1 g of toner was shown.

(F) Toner Scattering Copying was performed using a character original having an area ratio of the black portion of 8%.
At the time of copying 50,000 sheets (at that time when the transfer efficiency has become less than 70%), the toner scattering state in the copying machine was visually observed and evaluated according to the following criteria. ○: No toner scattering ×: Toner scattering

(G) Durability Copying was performed using a character original having an area ratio of the black portion of 8%.
The toner transfer efficiency was calculated from the toner consumption amount for every 10,000 copies and the collected toner amount. The durability was evaluated by the number of copies when the transfer efficiency first became less than 70%.

(H) Spent amount Copying is performed using a character original having an area ratio of black portion of 8%,
The developer was sampled at the time of copying 50,000 sheets (at that time when the transfer efficiency was less than 70%). This developer is placed on a 400-mesh screen and sucked from below by a blower to separate the toner from the carrier. 5 g of the carrier remaining on the sieve is put into a beaker, and toluene is further added to the beaker, and spent to dissolve the toner adhering to the surface of the carrier. Then, the toluene solution is dropped from under the beaker while the carrier is attracted by the magnet. After repeating this several times until the toluene becomes colorless, the toluene is dried in an oven and the weight is measured. The difference between the weight put in the beaker and the weight after drying is the amount of spent. The amount of spent is expressed in mg of spent toner attached to 1 g of carrier.

(Production Example 1: Production of fixing resin medium) Mixture containing styrene, butyl methacrylate and acrylic acid in a weight ratio of 80: 15: 5 Mixture 10
0 parts by weight, polypropylene wax (average molecular weight: 4,
000) 0.6 part by weight and a polymerization initiator were mixed in a soluble solvent and stirred to dissolve. The resulting mixed solution is put into a reaction kettle and stirred well with a stirring blade at 150 ° C / 5.
Polymerization was performed for a period of time, and then the reaction solution was degassed and dried to obtain a low molecular weight polymer containing a component to which polypropylene wax was graft-fixed.

Mixture containing 100 parts by weight of the low molecular weight polymer obtained above, styrene, butyl methacrylate and acrylic acid in a weight ratio of 70: 25: 5 1
00 parts by weight, the same polypropylene wax as above 5.4
Parts by weight, a polymerization initiator, mixed with a soluble solvent and stirred,
A mixed solution was prepared. Charge this mixed solution into the reaction kettle,
Polymerization was carried out at 80 ° C. for 15 hours while stirring well with a stirring blade, and then the reaction solution was degassed and dried to obtain the desired fixing resin. The acid value of this fixing resin was 10. The GPC molecular weight curve of this fixing resin is shown in FIG. As is clear from this figure, with this fixing resin,
It had a molecular weight peak at 10,000 and a molecular weight distribution on the higher molecular weight side, and the weight average molecular weight of this fixing resin was 100,000.

(Example 1) The following components: 103 parts by weight of the fixing resin obtained in Preparation Example 1 (3 parts by weight of wax) 10 parts by weight of carbon black [pH: 3.5, (7-pH) / specific surface area ( m ^{2 /} g): 0.025, acid treatment with nitric acid] 2 parts by weight of magnetite (magnetic powder) was melt-kneaded by a twin-screw extruder, and then this kneaded material was pulverized by a jet mill and classified by an air classifier. 10.0 μm
Particles were obtained. With respect to 100 parts by weight of the particles, 0.3 part by weight of hydrophobic silica fine particles having an average particle size of 0.015 μm as a fluidity improving agent and an average particle size of 0.
0.6 parts by weight of 3 μm alumina particles were externally added and mixed with a Henschel mixer to obtain a toner. The above toner was mixed with a ferrite carrier having an average particle size of 100 μm to obtain a two-component developer having a toner concentration of 3.5% by weight.

(Comparative Example 1) In Preparation Example 1, a fixing resin was manufactured without using polypropylene wax at all. Example 1 except that 100 parts by weight of this fixing resin and 3 parts by weight of the polypropylene wax used in Production Example 1 were used.
A toner and a two-component developer were prepared in exactly the same manner as in.

(Comparative Example 2) As carbon black, p
H = 9, (7-pH ) / specific surface area ^{(m 2 / g) = -} 0.
A toner and a developer were prepared in exactly the same manner as in Example 1 except that 013 which was not treated with an acid was used.

Table 1 shows the evaluation of the developers of Example 1 and Comparative Examples 1 and 2 described above.

[0097]

[Table 1]

Example 2 1000 parts by weight of spherical ferrite particles having an average particle size of 100 μm, 3.5 parts by weight of styrene-acrylic resin and 1.5 parts by weight of methylated melamine resin were added to 200 parts by weight of toluene. The mixture was added to and mixed with the dissolved coating liquid, and the mixture was heated and stirred, the solvent (toluene) was dried and removed from the obtained mixture, and further heat-treated at 200 ° C. for 1 hour to obtain resin-coated carrier particles. A two-component magnetic developer having a toner concentration of 3.5% by weight was obtained in the same manner as in Example 1 except that the resin-coated carrier particles were used.

Example 3 Amino group-containing styrene-acrylic resin 100 parts by weight Magnetite (magnetic powder) 400 parts by weight Carbon black (pH = 9) 5 parts by weight was melt-kneaded by a twin-screw extruder, and then this kneading. The product was crushed by a jet mill and classified by an air classifier to obtain 80 μm binder type carrier particles. A two-component magnetic developer having a toner concentration of 5.0% by weight was obtained in exactly the same manner as in Example 1 except that the binder type carrier particles in which the magnetic powder was dispersed in the resin were used.

Table 2 shows the evaluation results of the developers prepared in Examples 2 and 3 above.

[0101]

[Table 2]

As can be understood from the evaluation results shown in Tables 1 and 2, the developers of Examples 1 to 3 have good toner scattering and durability, but the developers of Comparative Example 1 have good results. The durability is poor, and in Comparative Example 2, the durability is deteriorated and the toner scattering is increased.

[0103]

According to the present invention, in a two-component magnetic developer toner, a copolymer resin or resin composition having an anionic polar group is used as a fixing resin medium and dispersed in the resin medium. The carbon black to be used has a pH of less than 7 and a ratio of (7-pH) / specific surface area of 0.010.
If the amount of the charge control agent is 0.050 to 0.050, it is possible to secure a sufficient toner charge amount for development without blending with a negative charge control agent, and transfer of the charge control agent to the carrier surface and charge due to this spent. The defects can be eliminated, the charging performance of the toner can be stabilized for a long time, and the life of the toner and the carrier can be extended.

Further, by containing a polymer component having a wax graft-fixed in the fixing resin medium, it becomes possible to uniformly disperse the wax, whereby stable image quality can be continuously exhibited. I was able to.

[Brief description of drawings]

Figure 1: Chromium complex salt dye (2: 1 type) as charge control agent
3 is an absorbance curve at a wavelength of 200 to 700 nm of an extraction liquid obtained by extracting a toner containing a toner with methanol.

FIG. 2 Wavelength 200 to 700 nm of a methanol extract of toner using a salicylic acid metal complex as a charge control agent.
It is an absorbance curve in.

FIG. 3 is a diagram showing the carrier used in the measurement of FIG. 1 as a two-component magnetic developer, and a carrier in which a charging failure has occurred due to spent is similarly extracted with methanol, and the absorbance of this extract at a wavelength of 200 to 700 nm. It is the graph which measured the curve.

FIG. 4 is a graph plotting the relationship between the mixing time and the amount of charge when a mixture of a toner containing a positive charge control agent and a magnetic carrier and a mixture of a toner containing no charge control agent and a magnetic carrier are mixed. Is.

FIG. 5 is a graph plotting the relationship between the mixing time and the charge amount when a mixture of a toner containing a negative charge control agent and a magnetic carrier and a mixture of a toner not containing a charge control agent and a magnetic carrier are mixed. Is.

FIG. 6 is a graph showing the relationship between the amount of spent spent carrier and the amount of charge control agent in spent toner.

FIG. 7 is a graph showing the relationship between the mixing time and the charge amount when the individual components in the toner are mixed with the magnetic carrier.

FIG. 8 is an explanatory diagram illustrating the occurrence of charging failure due to spent generation in a conventional two-component magnetic developer.

FIG. 9 is an absorbance curve at a wavelength of 200 to 700 nm in an extract obtained by extracting the negatively chargeable toner of the present invention with methanol.

10 is a GPC molecular weight distribution curve of a fixing resin medium used in the toner of the present invention manufactured in Example 1. FIG.

─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. ⁶ Identification number Internal reference number FI Technical display location G03G 9/113 G03G 9/08 371 9/10 331 351 (72) Inventor Shimizu Yoshio Osaka City Central Ward 1-22, Mita Kogyo Co., Ltd. (72) Inventor Kazuya Nagao Chuo-ku, Osaka 1-2-2 Tamazo, Mita Kogyo Co., Ltd. (72) Inventor Tomohide Iida Chuo-ku, Osaka 1-22 Tamatsukuri Mita Engineering Co., Ltd. (72) Inventor Eiichi Tamura 1-2-2 Tamatsukuri Chuo-ku, Osaka City Mita Engineering Co., Ltd.

Claims (12)

[Claims] 1. A negatively charging two-component magnetic developer toner comprising carbon black dispersed in a fixing resin medium, wherein the fixing resin medium is a free or neutralized anionic polar group. And a polymer component having a wax graft-fixed thereto, wherein the carbon black has a pH of less than 7 and (7-p
H) / specific surface area (m ² / g) is 0.010 to 0.05
0 to 4 and 1 to 4 per fixing resin medium
A toner for a two-component magnetic developer, which is blended in an amount of 5% by weight. 2. The toner according to claim 1, wherein the absorbance of the extract obtained by extracting the toner with methanol is substantially zero in the wavelength region of 400 to 700 nm and has no absorption peak in the region of 280 to 350 nm. 3. The toner according to claim 1, wherein the fixing resin medium has an acid value of an anionic polar group measured in the form of a free acid in the range of 4 to 30. 4. The toner according to claim 1, wherein the graft-fixed wax is contained in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the fixing resin medium. 5. The toner according to claim 1, wherein the wax graft fixing polymer component has the anionic polar group. 6. The toner according to claim 1, wherein the wax graft fixing polymer component is blended with the copolymer resin having the anionic polar group. 7. The copolymer resin having an anionic polar group is a styrene-acrylic copolymer resin.
The toner according to. 8. The fixing resin medium has a weight average molecular weight in the range of 70,000 to 200,000, and 4,000 to 3
The toner according to claim 1, which has a molecular weight peak in the range of 10,000. 9. The toner is composed of particles having a volume-based average particle diameter of 5 to 15 μm, and spacer particles having a volume-based average particle diameter of 0.05 to 1.0 μm are attached to the surface of the particles. The toner according to claim 1, wherein 10. The toner according to claim 1, wherein 0.1 to 5 parts by weight of magnetic powder is dispersed in 100 parts by weight of the resin medium in the fixing resin medium. 11. A two-component magnetic developer comprising the toner according to claim 1 and a resin-coated magnetic carrier. 12. A two-component magnetic developer comprising the toner according to claim 1 and a magnetic carrier in which magnetic powder is dispersed in a resin.